Linked Data
dbSNP Id:
rs1557271025
gnomAD v2:
X-154065854-GTGCTGCA-G
MyVariant Identifiers:
chrX:g.154065855_154065861del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154837580_154837586del , CM000685.2:g.154837580_154837586del | GRCh38 |
| NC_000023.10:g.154065855_154065861del , CM000685.1:g.154065855_154065861del | GRCh37 |
| NC_000023.9:g.153719049_153719055del | NCBI36 |
| NG_011403.1:g.190138_190144del | |
| NG_033065.1:g.2077_2083del | |
| NG_011403.2:g.190138_190144del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.*11_*17del MANE Select | ENSP00000353393.4:n.*11_*17del | |
| ENST00000644698.1:c.*11_*17del | ENSP00000495706.1:n.*11_*17del | |
| ENST00000330287.10:c.*11_*17del | ENSP00000327895.6:n.*11_*17del | |
| ENST00000360256.8:c.*11_*17del | ENSP00000353393.4:n.*11_*17del | |
| NM_000132.3:c.*11_*17del | NP_000123.1:n.*11_*17del | |
| NM_019863.2:c.*11_*17del | NP_063916.1:n.*11_*17del | |
| XM_011531126.1:c.*11_*17del | XP_011529428.1:n.*11_*17del | |
| NM_000132.4:c.*11_*17del MANE Select | NP_000123.1:n.*11_*17del | |
| NM_019863.3:c.*11_*17del | NP_063916.1:n.*11_*17del |